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Clinical Applications of PCR

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Cover of 'Clinical Applications of PCR'

Table of Contents

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    Book Overview
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    Chapter 1 A Targeted Q-PCR-Based Method for Point Mutation Testing by Analyzing Circulating DNA for Cancer Management Care.
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    Chapter 2 COLD-PCR: Applications and Advantages
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    Chapter 3 PCR-Based Detection of DNA Copy Number Variation.
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    Chapter 4 Emulsion PCR: Techniques and Applications
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    Chapter 5 Digital PCR: Principles and Applications
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    Chapter 6 Quantitative PCR for Plasma Epstein-Barr Virus Loads in Cancer Diagnostics
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    Chapter 7 High-Resolution Melt Curve Analysis in Cancer Mutation Screen
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    Chapter 8 Locked Nucleic Acid Probes (LNA) for Enhanced Detection of Low-Level, Clinically Significant Mutations
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    Chapter 9 Genotyping of Frequent Mutations in Solid Tumors by PCR-Based Single-Base Extension and MassARRAY Analysis
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    Chapter 10 Microfluidics-Based PCR for Fusion Transcript Detection.
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    Chapter 11 Polymerase Chain Reaction Diagnosis of Leishmaniasis: A Species-Specific Approach
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    Chapter 12 Detection of Trypanosoma cruzi by Polymerase Chain Reaction
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    Chapter 13 PCR Techniques in Next-Generation Sequencing.
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    Chapter 14 Single-Cell Quantitative PCR: Advances and Potential in Cancer Diagnostics
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    Chapter 15 Quantitative Real-Time PCR: Recent Advances
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    Chapter 16 PCR Techniques in Characterizing DNA Methylation.
Attention for Chapter 5: Digital PCR: Principles and Applications
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Chapter title
Digital PCR: Principles and Applications
Chapter number 5
Book title
Clinical Applications of PCR
Published in
Methods in molecular biology, February 2016
DOI 10.1007/978-1-4939-3360-0_5
Pubmed ID
Book ISBNs
978-1-4939-3358-7, 978-1-4939-3360-0
Authors

Kanagal-Shamanna, Rashmi, Rashmi Kanagal-Shamanna

Editors

Rajyalakshmi Luthra, Rajesh R. Singh, Keyur P. Patel

Abstract

Digital PCR is a robust PCR technique that enables precise and accurate absolute quantitation of target molecules by diluting and partitioning of the samples into numerous compartments. Automated partitioning can be attained by creating "water-in-oil" emulsion (emulsion-based digital PCR) or using a chip with microchannels (microfluidics-based digital PCR). We discuss the advantages and a wide variety of clinical applications of this technique. We describe the droplet digital RT-PCR protocol published by Jennings et al. for identification and absolute quantitation of BCR-ABL1 transcripts.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 128 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Malaysia 1 <1%
Mexico 1 <1%
Sweden 1 <1%
Brazil 1 <1%
Unknown 124 97%

Demographic breakdown

Readers by professional status Count As %
Student > Master 18 14%
Student > Bachelor 18 14%
Researcher 11 9%
Student > Ph. D. Student 11 9%
Other 8 6%
Other 18 14%
Unknown 44 34%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 30 23%
Engineering 14 11%
Agricultural and Biological Sciences 8 6%
Medicine and Dentistry 8 6%
Computer Science 3 2%
Other 15 12%
Unknown 50 39%